Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Fatemeh Shakarami"'
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 10, Iss 10, Pp n/a-n/a (2022)
Abstract Background X‐linked mental retardation‐hypotonic facies syndrome‐1 (MRXFH1), caused by a mutation in the ATRX gene, is a rare syndromic form of X‐linked mental retardation (XLMR) that is mainly characterized by severe intellectual di
Externí odkaz:
https://doaj.org/article/925f65b536c6485ba12a20f03e0c292b
Publikováno v:
Iranian Journal of Reproductive Medicine, Vol 13, Iss 10, Pp 627-632 (2015)
Background: Recurrent pregnancy loss (RPL) defined by two or more failed pregnancies before 20 weeks of gestation. Several factors play a role in RPL including thrombophilic conditions which can be influenced by gene polymorphisms. Plasminogen activa
Externí odkaz:
https://doaj.org/article/2b0b88b8699741b1b3f269b0400f424d
Publikováno v:
Gene, Cell and Tissue. 3
Background: Recurrent pregnancy loss (RPL) is two or more consecutive pregnancy losses before 20 weeks of gestation. So far the disease is known for a variety of reasons, but still about 50% of recurrent pregnancy losses are unknown. The miRNAs are a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::59b2c414bd052209b385fee211813b75
https://doi.org/10.17795/gct-34526
https://doi.org/10.17795/gct-34526